Intramolecular carbolithiation and palladium-catalyzed c-c bond forming reactions in the construction of medium sized rings. Selective synthesis of fused indolizine, pyrroloazepine and pyrroloazocine

  1. COYA DIAZ DE SARRALDE, ESTIBALIZ
unter der Leitung von:
  1. María Nuria Sotomayor Anduiza Doktormutter
  2. Maria Esther Lete Exposito Doktormutter

Universität der Verteidigung: Universidad del País Vasco - Euskal Herriko Unibertsitatea

Fecha de defensa: 19 von Dezember von 2013

Gericht:
  1. José Luis García Ruano Präsident/in
  2. Antonia Mielgo Vicente Sekretärin
  3. Alessandro Mordini Vocal
  4. María Elena González Nuñez Vocal
  5. José Luis Vicario Hernando Vocal

Art: Dissertation

Teseo: 116434 DIALNET

Zusammenfassung

The research work described in this thesis has focused on the develop`ment of new methods for he syntehesis of heterocycles using organolithium intermediates and palladium-catalyzed coupling reactions for the formation of carbon-carbon bonds.the intramolecular carbolithiation reactionor arylithiums has been extended to the construction of medium sized rings, and has also been applied to heteroaryllilthiums. Besides, the competion between Mizoreoki-Heck and direct arylation reaction in the construction of medium sized rings on both aromatic and heteroaromatic systems has been studied. In this context, the asymmetric version of mizoroki-heck reactions, as well as cascade processes have also been studied. Thus. efficient procedures for the obtention of fused indlizine, pyrroloazepine and pyrroloazocine systems have been developed.